FDA applicant

Intergrated Visual, Inc.

Quincy, IL1 decision1992–19920 recalls

FDA records 1 decision for Intergrated Visual, Inc. (Quincy, IL) in 1992: 1 510(k) clearance. All are in product code GES (Blade, Scalpel). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Intergrated Visual, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intergrated Visual, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Intergrated Visual, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Intergrated Visual, Inc.

Which product codes does it file in?

What has FDA decided for it lately?